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Autism associated with 12q (12q24.31-q24.33) deletion: further report of an exceedingly rare disorder
Chromosomal abnormalities are responsible for several congenital malformations in the world, some of these are associated to telomeric/subtelomeric deletions. The abnormalities involving the telomere of chromosome 12 are rare, with few reports of deletions involving 12q24.31 region in the literature...
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| Publié dans: | Einstein (Sao Paulo) |
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| Auteurs principaux: | , , , , , |
| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
Instituto Israelita de Ensino e Pesquisa Albert Einstein
2020
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| Sujets: | |
| Accès en ligne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7279891/ https://ncbi.nlm.nih.gov/pubmed/32578677 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.31744/einstein_journal/2020RC5335 |
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